Reactome | Mutational Signature Analysis Reveals NTHL1 Deficiency to Cause a Multi-tumor Phenotype

author	[Person:9637187] Grolleman, JE [Person:9629995] de Voer, RM [Person:9637182] Elsayed, FA [Person:9606202] Nielsen, M [Person:9637192] Weren, RDA [Person:9637173] Palles, C [Person:9637202] Ligtenberg, MJL [Person:9637200] Vos, JR [Person:9637175] Ten Broeke, SW [Person:9637179] de Miranda, NFCC [Person:9637170] Kuiper, RA [Person:9629989] Kamping, EJ [Person:9637184] Jansen, EAM [Person:9637174] Vink-B�rger, ME [Person:9637188] Popp, I [Person:9637176] Lang, A [Person:9637191] Spier, I [Person:9637197] H�neburg, R [Person:9637205] James, PA [Person:3927946] Li, N [Person:9637183] Staninova, M [Person:9637177] Lindsay, H [Person:9637171] Cockburn, D [Person:9637206] Spasic-Boskovic, O [Person:9637181] Clendenning, M [Person:9637196] Sweet, K [Person:9637204] Capell�, G [Person:9637172] Sjursen, W [Person:9637198] H�berg-Vetti, H [Person:9629994] Jongmans, MC [Person:5661069] Neveling, K [Person:9629998] Geurts van Kessel, A [Person:5632966] Morreau, H [Person:9606201] Hes, FJ [Person:9637190] Sijmons, RH [Person:9637189] Schackert, HK [Person:9637186] Ruiz-Ponte, C [Person:9637199] Dymerska, D [Person:2206343] Lubinski, J [Person:9630273] Rivera, B [Person:9630272] Foulkes, WD [Person:9605321] Tomlinson, IP [Person:3662204] Valle, L [Person:9637195] Buchanan, DD [Person:9637185] Kenwrick, S [Person:9637180] Adlard, J [Person:9637194] Dimovski, AJ [Person:2011520] Campbell, IG [Person:9637201] Aretz, S [Person:2429709] Schindler, D [Person:9637203] van Wezel, T [Person:9629993] Hoogerbrugge, N [Person:9629996] Kuiper, RP
created	[InstanceEdit:9637178] Orlic-Milacic, Marija, 2019-02-14
dbId	9637193
displayName	Mutational Signature Analysis Reveals NTHL1 Deficiency to Cause a Multi-tumor Phenotype
journal	Cancer Cell
pages	256-266.e5
pubMedIdentifier	30753826
schemaClass	LiteratureReference
title	Mutational Signature Analysis Reveals NTHL1 Deficiency to Cause a Multi-tumor Phenotype
url	http://www.ncbi.nlm.nih.gov/pubmed/30753826
volume	35
year	2019

Mutational Signature Analysis Reveals NTHL1 Deficiency to Cause a Multi-tumor Phenotype Show undefined attributes

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